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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00575458
Other study ID # 2005p002466
Secondary ID
Status Completed
Phase N/A
First received December 14, 2007
Last updated November 15, 2010
Start date June 2005
Est. completion date June 2010

Study information

Verified date November 2010
Source Massachusetts General Hospital
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This study is comparing two different kinds of splints for patients who have had a surgical contracture release of dupuytren's disease. It compares a static splint and a dynamic splint.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date June 2010
Est. primary completion date June 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years or older

- males and females with Dupuytren's contracture

- patients with contracture of less than 30 degrees of MCP contractions and no contractions of the IP joints

Exclusion Criteria:

- previous surgical treatment for Dupuytren's

- contracture of MCP greater than 30 degrees

- contraindications for dynamic splinting (upper limb amputees, paresis, ect.)

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Massachusetts General Hospital Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary DASH questionnaire, PCS questionnaire, Wahler Physical Symptom Inventory, CESD questionnaire 6 months No
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